rs1510552
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1510552(G;G) |
| Make rs1510552(G;T) |
| Make rs1510552(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 214052678 |
| Gene | SPAG16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1510552 |
| dbSNP (classic) | rs1510552 |
| ClinGen | rs1510552 |
| ebi | rs1510552 |
| HLI | rs1510552 |
| Exac | rs1510552 |
| Gnomad | rs1510552 |
| Varsome | rs1510552 |
| LitVar | rs1510552 |
| Map | rs1510552 |
| PheGenI | rs1510552 |
| Biobank | rs1510552 |
| 1000 genomes | rs1510552 |
| hgdp | rs1510552 |
| ensembl | rs1510552 |
| geneview | rs1510552 |
| scholar | rs1510552 |
| rs1510552 | |
| pharmgkb | rs1510552 |
| gwascentral | rs1510552 |
| openSNP | rs1510552 |
| 23andMe | rs1510552 |
| SNPshot | rs1510552 |
| SNPdbe | rs1510552 |
| MSV3d | rs1510552 |
| GWAS Ctlg | rs1510552 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24152035] |
| Trait | Contrast sensitivity |
| Title | Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia. |
| Risk Allele | |
| P-val | 1E-6 |
| Odds Ratio | 3.04 [NR] unit increase |
